Have questions? Visit https://www.reddit.com/r/SNPedia

rs587784558

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587784558(A;A)
Make rs587784558(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position36065984
GeneWDR62
is asnp
is mentioned by
dbSNPrs587784558
ebirs587784558
HLIrs587784558
Exacrs587784558
Varsomers587784558
Maprs587784558
PheGenIrs587784558
hapmaprs587784558
1000 genomesrs587784558
hgdprs587784558
ensemblrs587784558
gopubmedrs587784558
geneviewrs587784558
scholarrs587784558
googlers587784558
pharmgkbrs587784558
gwascentralrs587784558
openSNPrs587784558
23andMers587784558
23andMe allrs587784558
SNP Nexus

SNPshotrs587784558
SNPdbers587784558
MSV3drs587784558
GWAS Ctlgrs587784558
Max Magnitude0
ClinVar
Risk rs587784558(A;A)
Alt rs587784558(A;A)
Reference rs587784558(C;C)
Significance Probable-Pathogenic
Disease Primary autosomal recessive microcephaly 2
Variation info
Gene WDR62
CLNDBN Primary autosomal recessive microcephaly 2
Reversed 0
HGVS NC_000019.9:g.36556886C>A
CLNSRC
CLNACC RCV000147962.1,